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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >No genetic association between alpha-2 macroglobulin I1000V polymorphism and Japanese sporadic Alzheimer's disease.
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No genetic association between alpha-2 macroglobulin I1000V polymorphism and Japanese sporadic Alzheimer's disease.

机译:alpha-2巨球蛋白I1000V多态性与日本散发的阿尔茨海默氏病之间没有遗传关联。

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摘要

Alpha-2 macroglobulin (A2M) is a serum pan-protease inhibitor that is related with the pathogenesis of Alzheimer's disease (AD) through its ability to mediate amyloid beta degradation. Recently, it has been reported that the I1000V polymorphism in A2M gene might increase the risk of AD. In the present study, we investigated this mutation in 95 healthy controls and in 111 sporadic AD cases by polymerase chain reaction-restriction fragment length polymorphism method in order to study this hypothesis in the Japanese AD population. Allelic frequencies with the I1000V polymorphism in the gene were 7.4 and 6.8% in the control and AD groups, respectively. Our results failed to demonstrate an association between this polymorphism and Japanese sporadic AD, and the A2M I1000V mutation does not seem to be a risk factor per se for sporadic AD.
机译:Alpha-2巨球蛋白(A2M)是一种血清泛蛋白酶抑制剂,它通过介导淀粉样β降解的能力与阿尔茨海默氏病(AD)的发病机理有关。最近,有报道说A2M基因中的I1000V多态性可能会增加患AD的风险。在本研究中,我们通过聚合酶链反应-限制性片段长度多态性方法在95个健康对照和111个散发性AD患者中调查了此​​突变,以研究日本AD人群中的这一假设。对照组和AD组中具有I1000V基因多态性的等位基因频率分别为7.4和6.8%。我们的结果未能证明这种多态性与日本散发性AD之间存在关联,并且A2M I1000V突变似乎并不是散发性AD本身的危险因素。

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